Which are Compliant for Inspections for a [GXP Compliance]

MessageThis Webinar is over
Date Nov 12, 2018
Time 10:00 AM to 11:00 AM
Cost 150.00
Online
Overview:
This webinar will help Sponsors, CROs in the US, EU and 

internationally,understand how to write SOPs to comply with inspection 

requirements.

Why should you Attend:
This webinar will assist you to prepare for inspection of SOPs, particularly 

since such inspection readiness of SOPs are taking considerable time to 

prepare for. Inspections of SOPs of critical activities that impact business 

success on several levels. Therefore, preparation and management of the 

inspection and audit process of SOPs is an important business activity, not 

just a distraction from day to day routine. 

Areas Covered in the Session:
Understand why we need written SOP procedures
Gain an insight into expectations for an effective written documentation
Understand Regulatory requirements for the creation, compliance and 

maintenance of SOPs
Gain techniques for creating effective SOPs and other written documents 

to minimize costly revisions

Who Will Benefit:
Clinical Research Associates
Clinical Research Archiving and Document Management Personnel
Quality Assurance Managers and Auditors
Clinical Development Managers and Personnel
Manufacturing
Pharmacovigilance
Laboratories

Speaker Profile:
Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an independent 

QA and training consultant in the pharmaceutical industry. She is a 

managing director with LB Training and Development Ltd., course director 

for the M.Sc. in Clinical Research, School of Pharmacy at the University of 

Cardiff, and course director for M.Sc.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

 


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